| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22
|
Butterfield, Russell J.
|
|
2009
|
19 |
4 |
p. 279-287
9 p.
|
artikel
|
| 2 |
Characterization of the DMD/BMD patient population in Czech Republic and Slovakia using an innovative registry approach
|
Brabec, Petr
|
|
2009
|
19 |
4 |
p. 250-254
5 p.
|
artikel
|
| 3 |
Clinical and audiological follow up of a family with the 8363G>A mutation in the mitochondrial DNA
|
DiFabio, Roberto
|
|
2009
|
19 |
4 |
p. 291-296
6 p.
|
artikel
|
| 4 |
Demyelinating disease of central and peripheral nervous systems associated with a A8344G mutation in tRNALys
|
Erol, I.
|
|
2009
|
19 |
4 |
p. 275-278
4 p.
|
artikel
|
| 5 |
Editorial Board
|
|
|
2009
|
19 |
4 |
p. IFC-
1 p.
|
artikel
|
| 6 |
Eosinophilic myositis in calpainopathy: Could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease?
|
Oflazer, Piraye Serdaroglu
|
|
2009
|
19 |
4 |
p. 261-263
3 p.
|
artikel
|
| 7 |
George Karpati O.C., C.Q., M.D., FRCPC, FRS (C) 1934–2009
|
Eisen, Andrew
|
|
2009
|
19 |
4 |
p. 306-
1 p.
|
artikel
|
| 8 |
Late-onset seropositive Isaacs’ syndrome after Guillain–Barré syndrome
|
Myers, Kenneth A.
|
|
2009
|
19 |
4 |
p. 288-290
3 p.
|
artikel
|
| 9 |
Mammalian animal models for Duchenne muscular dystrophy
|
Willmann, Raffaella
|
|
2009
|
19 |
4 |
p. 241-249
9 p.
|
artikel
|
| 10 |
Phenotypic variability in giant axonal neuropathy
|
Tazir, Meriem
|
|
2009
|
19 |
4 |
p. 270-274
5 p.
|
artikel
|
| 11 |
161st ENMC International Workshop on nemaline myopathy and related disorders, Newcastle upon Tyne, 2008
|
Laing, Nigel G.
|
|
2009
|
19 |
4 |
p. 300-305
6 p.
|
artikel
|
| 12 |
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegia
|
Sotiriou, Evangelia
|
|
2009
|
19 |
4 |
p. 297-299
3 p.
|
artikel
|
| 13 |
The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy
|
Houlden, Henry
|
|
2009
|
19 |
4 |
p. 264-269
6 p.
|
artikel
|
| 14 |
Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H
|
Cossée, Mireille
|
|
2009
|
19 |
4 |
p. 255-260
6 p.
|
artikel
|
| 15 |
WMS 2009
|
|
|
2009
|
19 |
4 |
p. II-
1 p.
|
artikel
|
| 16 |
WMS News
|
|
|
2009
|
19 |
4 |
p. IV-V
nvt p.
|
artikel
|
| 17 |
WMS online application form
|
|
|
2009
|
19 |
4 |
p. III-
1 p.
|
artikel
|
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